Canonical Allele Identifier: CA337834329

Gene: AGRN

Linked Data

• dbSNP Id: rs1298122116
• gnomAD v2: 1-979211-G-C
• gnomAD v4: 1-1043831-G-C
• COSMIC: COSM308994
• MyVariant Identifiers: chr1:g.979211G>C (hg19) ; chr1:g.1043831G>C (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000001.11:g.1043831G>C , CM000663.2:g.1043831G>C	GRCh38
NC_000001.10:g.979211G>C , CM000663.1:g.979211G>C	GRCh37
NC_000001.9:g.969074G>C	NCBI36
NG_016346.1:g.28709G>C , LRG_198:g.28709G>C

Transcript Alleles

HGVS	Amino-acid Change
ENST00000379370.7:c.1807G>C MANE Select	ENSP00000368678.2:p.Gly603Arg
ENST00000651234.1:c.1492G>C	ENSP00000499046.1:p.Gly498Arg
ENST00000652369.1:c.1492G>C	ENSP00000498543.1:p.Gly498Arg
ENST00000379370.6:c.1807G>C	ENSP00000368678.2:p.Gly603Arg
ENST00000620552.4:c.1393G>C	ENSP00000484607.1:p.Gly465Arg
NM_001305275.1:c.1807G>C	NP_001292204.1:p.Gly603Arg
NM_198576.3:c.1807G>C	NP_940978.2:p.Gly603Arg
XM_005244749.2:c.1807G>C	XP_005244806.1:p.Gly603Arg
XM_006710635.2:c.1807G>C	XP_006710698.1:p.Gly603Arg
XM_011541429.1:c.1807G>C	XP_011539731.1:p.Gly603Arg
XM_011541430.1:c.934G>C	XP_011539732.1:p.Gly312Arg
XM_011541431.1:c.73G>C	XP_011539733.1:p.Gly25Arg
XR_946650.1:n.1874G>C
NM_001364727.1:c.1492G>C	NP_001351656.1:p.Gly498Arg
XM_005244749.3:c.1807G>C	XP_005244806.1:p.Gly603Arg
XM_011541429.2:c.1807G>C	XP_011539731.1:p.Gly603Arg
XR_946650.2:n.1878G>C
NM_001305275.2:c.1807G>C	NP_001292204.1:p.Gly603Arg
NM_198576.4:c.1807G>C MANE Select	NP_940978.2:p.Gly603Arg
NM_001364727.2:c.1492G>C	NP_001351656.1:p.Gly498Arg